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All of the informants spoke Swedish and were thoroughly informed about the aim of the study.
Women were informed about the aim of the study and information about anonymity, confidentiality, and consent was included in the explanation.
All patients informed about the aim of the study and their informed consent was obtained.
All patients were informed about the aim of the study and signed an informed consent.
All of the subjects were volunteers; they were informed about the aim of the study and gave written informed consent before the study began.
Prior to the initiation of the study, each subject was informed about the aim of the study and signed an informed consent form.
All participants were informed about the aim of the study, gave their written informed consent (on a separate sheet of paper from the questionnaire) and participated on a strictly voluntary basis.
Homozygous and heterozygous FH patients with documented genetic defects in the LDL receptor (LDLR) gene and healthy volunteers were informed about the aim of the study and gave written informed consent.
All patients were informed about the aim and procedures of the study and written informed consent was obtained from all participants.
The subjects were informed about the aim of this study.
Participants were informed about the aim of the study and that their participation was anonymous and voluntary.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com